Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
  • C07C41/01—Preparation of ethers
  • C07C41/02—Preparation of ethers from oxiranes
  • C07C41/03—Preparation of ethers from oxiranes by reaction of oxirane rings with hydroxy groups
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C43/00—Ethers; Compounds having groups, groups or groups
  • C07C43/02—Ethers
  • C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
  • C07C43/04—Saturated ethers
  • C07C43/10—Saturated ethers of polyhydroxy compounds
  • C07C43/11—Polyethers containing —O—(C—C—O—)n units with ≤ 2 n≤ 10
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
  • C11D1/66—Non-ionic compounds
  • C11D1/825—Mixtures of compounds all of which are non-ionic
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
  • C11D1/66—Non-ionic compounds
  • C11D1/83—Mixtures of non-ionic with anionic compounds
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
  • C11D1/66—Non-ionic compounds
  • C11D1/72—Ethers of polyoxyalkylene glycols
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
  • C11D1/66—Non-ionic compounds
  • C11D1/722—Ethers of polyoxyalkylene glycols having mixed oxyalkylene groups; Polyalkoxylated fatty alcohols or polyalkoxylated alkylaryl alcohols with mixed oxyalkylele groups

Definitions

• Alkoxylated alcohols and their use in formulations for hard surface cleaning are Alkoxylated alcohols and their use in formulations for hard surface cleaning
• the present invention is directed towards the formulations, comprising at least one compound according to general formula (I) wherein the integers R 1 are different or identical and selected from C3-Cio-alkyl groups with at least two methyl groups per R 1 ,
• AO being selected from -CH2CH2O- and CH2CH(R 2 )0- and being different or identical in the case of n > 1 R 2 being different or identical and selected from Ci-Ci6-alkyl, branched or linear, n in the range of from 1 to 30,
• inventive formulations comprising at least one compound according to formula (I), to compounds according to formula (I), and to a process for manufacturing inventive compounds and inventive formulations.
• One task is to solubilize the dirt that is supposed to be removed and to keep it in the aqueous medium.
• Another task is to allow the aqueous medium to at all come into contact with the surface to be cleaned. Such a contact can be prevented, e. g., due to the high surface tension of water. Instead of a good wetting of the surface to be cleaned one observes bubbles of air sitting on such a surface and preventing the access of water to the re- spective surface.
• wetting agents are being employed.
• Such wetting agents can be selected from surfactants which serve a dual purpose: to reduce the sur- face tension of the water and to prevent bubbles of air remaining on the surface.
• WO 201 1/003904 a formulation has been disclosed that comprises an alkoxylated long-chain alcohol and an alkoxylated branched C8-Ci2-alcohol. They show good wetting and soil solubiliz- ing behavior. However, in certain applications such as tiles that are exposed to heat, residual soil can be observed. Tiles such as many other hard surfaces need thorough cleaning. Depending on where such tiles or other hard surfaces are located, e. g., in bath rooms, kitchens, hospitals, or the like, clean surfaces also mean good hygienic properties. Residual soil, to the contrary, can mean danger of non-hygienic environment.
• Formulations according to the invention comprise at least one compound according to general formula (I) wherein the integers are defined as follows:
• R 1 different or preferably identical and selected from C3-Cio-alkyl groups with at least two methyl groups per R 1 , for example three or four methyl groups per R 1 , such as tert. -butyl, preferably two methyl groups R 1 , such as iso-butyl, iso-pentyl, iso-hexyl, iso-dodecyl, and even more preferably iso-propyl, that is CH(CH3)2-groups.
• AO being selected from -CH2CH2O- and -CH2CH(R 2 )0- and being different or identical in the case of n > 1.
• the group -CH2CH2O- can also be abbreviated as EO in the context of the present invention.
• YH is selected from -[CH2CH(R 2 )0] y -[EO] x , with x being selected from 1 to 30, preferably 1 .5 to 15, even more preferably 2 to 10, and y being selected from zero to 5, preferably zero to 2 or 1 to 2.
• YH is selected from -[EO] x -[CH2CH(R 2 )0] y , with x being selected from 1 to 30, preferably 1 .5 to 15, even more preferably 2 to 10, and y being selected from zero to 5, preferably zero to 2.
• the integers x and y are average values in the context of the present invention, preferably number average.
• YH is selected from (AO) n , AO being identical and selected from -CH 2 CH 2 0- and -CH 2 CH(R 2 )0-, preferably EO.
• R 2 are different or identical and selected from Ci-Ci6-alkyl, branched or linear, preferably linear, more preferably n-propyl, ethyl and even more preferably methyl.
• n is in the range of from 1 to 30.
• the integer n is an average value in the context of the pre- sent invention, preferable number average values for n are 1.5 to 15, even more preferred
• the polydispersity (M w /M n ) of compound according to general formula (I) is in the range of from 1 .0 to 1 .5.
• inventive formulations contain in the range of from 0.01 to 95 % by weight compound of general formula (I), percentages being based on total weight of inventive formulations. In one embodiment of the present invention, inventive formulations contain in the range of from 2 to 50 % by weight, preferably 3 to 20 % by weight of compound of general formula (I). Such inventive formulations can be used as, e.g., bathroom cleaners, industrial hard surface cleaners, and kitchen cleaners. In one embodiment of the present invention, inventive formulations contain in the range of from 0.01 to 15 % by weight, preferably 0.02 to 7.5 % by weight of compound of general formula (I). Such inventive formulations can be used as, e.g., glass cleaners, and especially window cleaners.
• inventive formulations can also contain at least one compound according to the general formula (IV) wherein the integers are defined as follows R 3 are different or identical and selected from non-branched C3-Cio-alkyl groups with the same number of carbon atoms as R 1 in the corresponding compound of general formula (I), in other words, compounds of general formulae (I) and (IV) in the respective inventive formulation being isomers.
• R 3 are different or identical and selected from non-branched C3-Cio-alkyl groups with the same number of carbon atoms as R 1 in the corresponding compound of general formula (I), in other words, compounds of general formulae (I) and (IV) in the respective inventive formulation being isomers.
• inventive formulations can contain at least one compound according to general formulae (V a to (V c))
• inventive formulations contain
• inventive formulations can be solid, liquid or in the form of slurries.
• inventive formulations are selected from liquid and solid formulations.
• inventive formulations are aqueous, preferably liquid aqueous formulations.
• inventive formulations can contain 0.1 to 90 % by weight of water, based on total of the respective formulation.
• inventive formulations have a pH value in the range of from zero to 14, preferably from 2.5 to 1 1 .
• the pH value can be chosen according to the type of hard surface and the specific application. It is, e.g., preferred to select a pH value in the range of from 1 or less up to 2.5 for bathroom or toilet cleaners. It is furthermore preferred to select a pH value in the range of from 4 to 10 for dishwashing or floor cleaners.
• inventive formulations contain at least one active ingredient.
• Active ingredients can be selected from soaps, anionic surfactants, such as LAS (linear alkylbenzenesulfonate) or paraffine sulfonates or FAS (fatty alcohol sulfates) or FAES (fatty alcohol ether sulfates), furthermore acids, such as phosphoric acid, amidosulfonic acid, citric acid, lactic acid, acetic acid, other organic and inorganic acids, furthermore organic solvents, such as butyl glycol, n-butoxypropanol, especially 1 -butoxy-2-propanol, ethylene glycol, propylene glycol, glycerine, ethanol, monoethanolamine, and isopropanol.
• inventive formulations comprise at least one organic acid, selected from acetic acid, citric acid, and methanesulfonic acid.
• inventive formulations contain at least one or more active ingredients selected from non-ionic surfactants which are different from compounds of formulae (I) and (IV).
• suitable non-ionic surfactants are alkoxylated n-Ci2-C2o-fatty alcohols, such as n-Cio-C2o-alkyl(EO) m OH with m being in the range of from 5 to 100, furthermore block copolymers of ethylene oxide and propylene oxide, such as poly-EO-poly-PO-poly- EO with Mw in the range of from 3,000 to 5,000 g/mol PO content of from 20 to 50% by mass, furthermore alkyl polyglycosides, preferably branched Cs-do-alkyl polyglucosides, especially Cs-Cio-alkyl polyglucosides with a branching in 2-position of the respective Cs-do-alkyl group.
• inventive formulations can be used as bath cleaners, as sanitary cleaners, as kitchen cleaners, as toilet cleaners, as toilet bowl cleaners, as sanitary descalers, as all-purpose household cleaners, as all-purpose household cleaner concen- trates, as metal degreasers, as all purpose-household spray cleaners, as hand dish cleaners, as automatic dishwashing agents, or floor cleaners, as hand cleaners.
• inventive formulations can contain at least one bio- cide or preservative, such as benzalkonium chlorides.
• inventive formulations can be used as laundry detergents.
• inventive formulations can contain one or more active ingredients selected from inorganic builders such as phosphates, such as triphosphates.
• Phosphate-free formulations according to the present invention are preferred.
• the term "phosphate-free” refers to formulations with 0.5 % by weight of phosphate maximum, based on the total solids content and measured by gravimetric methods, and phosphate-free formulations can contain a minimum of 50 ppm (weight) phosphate or less.
• silicates examples include silicates, silicates, carbonates, and alumosilicates.
• Silicates and alumosilicates can be selected from crystalline and amorphous materials.
• inorganic builders are selected from crystalline alu- mosilicates with ion-exchanging properties, such as, in particular, zeolites.
• zeolites Various types of zeolites are suitable, in particular zeolites A, X, B, P, MAP and HS in their Na form or in forms in which Na is partially replaced by cations such as Li + , K + , Ca 2+ , Mg 2+ or ammonium.
• Suitable crystalline silicates are, for example, disilicates and sheet silicates.
• Crystalline silicates can be used in the form of their alkali metal, alkaline earth metal or ammonium salts, preferably as Na, Li and Mg silicates.
• Amorphous silicates such as, for example, sodium metasilicate, which has a polymeric structure, or Britesil ® H20 (manufacturer: Akzo) can be selected.
• Suitable inorganic builders based on carbonate are carbonates and hydrogencarbonates.
• Carbonates and hydrogencarbonates can be used in the form of their alkali metal, alkaline earth metal or ammonium salts.
• Na, Li and Mg carbonates or hydrogencarbonates, in particular sodium carbonate and/or sodium hydrogencarbonate can be selected.
• Other suitable inorganic builders are sodium sulphate and sodium citrate.
• inventive formulations can contain at least one organic complexing agent (organic cobuilders) such as EDTA ( ⁇ , ⁇ , ⁇ ', ⁇ '- ethylenediaminetetraacetic acid), NTA ( ⁇ , ⁇ , ⁇ -nitrilotriacetic acid), MGDA (2-methylglycine-N,N- diacetic acid), GLDA (glutamic acid ⁇ , ⁇ -diacetic acid), and phosphonates such as 2- phosphono-1 ,2,4-butanetricarboxylic acid, aminotri(methylenephosphonic acid), 1 - hydroxyethylene(1 ,1 -diphosphonic acid) (HEDP), ethylenediaminetetramethylenephosphonic acid, hexamethylenediaminetetramethylenephosphonic acid and diethylenetriaminepentameth- ylenephosphonic acid and in each case the respective alkali metal salts, especially the respec- tive sodium salts.
• organic cobuilders such as EDTA ( ⁇ , ⁇ , ⁇ '
• inventive formulations can contain one or more active ingredients selected from organic polymers, such as polyacrylates and copolymers of maleic acid-acrylic acid.
• inventive formulations can contain one or more active ingredients selected from alkali donors, such as hydroxides, silicates, carbonates.
• inventive formulations can contain one or more further ingredients such as perfume oils, oxidizing agents and bleaching agents, such as perborates, peracids or trichloroisocyanuric acid, Na or K dichloroisocyanurates, and enzymes.
• Most preferred enzymes include lipases, amylases, cellulases and proteases.
• esterases pectinases, lactases and peroxidases.
• Enzyme(s) may be deposited on a carrier substance or be encapsulated in order to protect them from premature decomposition.
• inventive formulations can contain one or more active ingredients such as graying inhibitors and soil release polymers.
• Suitable soil release polymers and/or graying inhibitors are:
• suitable soil release polymers are amphiphilic copolymers, especially graft copolymers of vinyl esters and/or acrylic esters onto polyalkylene oxides.
• inventive formulations can contain one or more active ingredients selected from dye transfer inhibitors, for example homopolymers and copolymers of vinylpyrrolidone, of vinylimidazole, of vinyloxazolidone or of 4-vinylpyridine N-oxide, each having average molar masses M w of from 15,000 to 100,000 g/mol, and cross-linked finely divided polymers based on the above monomers;
• dye transfer inhibitors for example homopolymers and copolymers of vinylpyrrolidone, of vinylimidazole, of vinyloxazolidone or of 4-vinylpyridine N-oxide, each having average molar masses M w of from 15,000 to 100,000 g/mol, and cross-linked finely divided polymers based on the above monomers;
• inventive formulations contain 0.1 to 50% by weight, preferably 1 to 20 % by weight organic complexing agent, based on the total solids content of the respective inventive formulation. In one embodiment of the present invention, inventive formulations contain 0.1 to 80% by weight, preferably 5 to 55 % by weight anionic surfactant, based on the total solids content of the respective inventive formulation. In one embodiment of the present invention, inventive formulations can contain one or more active ingredients selected from defoamers. Examples of suitable defoamers are silicon oils, especially dimethyl polysiloxanes which are liquid at room temperature, without or with silica particles, furthermore microcrystalline waxes and glycerides of fatty acids.
• inventive formulations do not contain any defoamer which shall mean in the context of the present invention that said inventive formulations comprise less than 0.1 % by weight of silicon oils and less than 0.1 % by weight of glycerides of fatty acids and less than 0.1 % by weight of microcrystalline waxes, referring to the total solids content of the respective inventive formulation, and in the extreme, no measureable amounts of silicon oils glycerides of fatty acids at all.
• formulations disclosed in WO 201 1/003904 can produce a certain amount of foam that is disadvantageous in various applications.
• the foam can transport soil to places not being easy to access and there it remains, together with the residual foam. Said residual foam may be due to incomplete rinsing.
• Inventive formulations show an extremely good performance when using them for cleaning hard surfaces, in particular tiles.
• a further aspect of the present invention is the use of inventive formulations for hard surface or fiber cleaning.
• a further aspect of the present invention is a method for cleaning hard surfaces under application of inventive formulations, hereinafter also briefly referred to as inventive cleaning method.
• Hard surfaces as used in the context with the present invention are defined as surfaces of water-insoluble and - preferably - non-swellable materials.
• Hard surfaces as used in the context of the present invention preferably also exhibit resistance against manual destruction such as scratching with fingernails. Preferably, they have a Mohs hardness of 3 or more.
• hard surfaces are glassware, tiles, stone, china, enamel, concrete, leather, steel, other metals such as iron or aluminum, furthermore wood, plastic, in particular melamine resins, polyethylene, polypropylene, PMMA, polycarbonates, polyesters such as PET, furthermore polystyrene and PVC, and furthermore, silicon (wafers) surfaces.
• inventive formulations when used for cleaning hard surfaces that are at least part of structured objects.
• structured objects refer to objects having, e. g. convex or concave elements, notches, furrows, corners, or elevations like bumps.
• Fibers as used in the context with the present invention can be of synthetic or natural origin.
• fibers of natural origin are cotton and wool.
• fibers of synthetic origin are polyurethane fibers such as Spandex® or Lycra®, polyester fibers, polyamide fibers, and glass wool.
• Other examples are biopolymer fibers such as viscose, and technical fibers such as GoreTex®.
• Fibers may be single fibers or parts of textiles such as knitwear, wovens, or nonwovens.
• inventive formulations are being applied.
• inventive formulations are applied in their embodiments as aqueous formulations, comprising, e. g., 10 to 99.9 % by weight water.
• Inventive formulations can be dispersions, solutions, gels, or solid blocks, emulsions including microemulsions, and foams, preferred are solu- tions. They can be used in highly diluted form, such as 1 :10 up to 1 :50.
• any hard surface or fiber or arrangement of fibers can be contacted (brought into contact) with an inventive formulation.
• inventive formulations can be applied at ambient temperature.
• inventive formulations can be used at elevated temperatures, such as 30 to 85°C, for examples by using an inventive formulation that has a temperature of 30 to 85°C, or by applying an inventive formulation to a preheated hard surface, e. g., preheated to 30 to 85°C.
• inventive formulation it is possible to apply an inventive formulation to a hard surface under normal pressure. In a further embodiment, it is possible to apply inventive formulation to a hard surface under pressure, e. g., by use of a high-pressure cleaner or a pressure washer.
• application duration of inventive formulation can be in the range of from one second up to 24 hours, preferably in the range of 30 min to 5 hours in the case of fiber cleaning and preferably one second up to 1 hour in cases such as floor cleaning, kitchen cleaning or bathroom cleaning.
• Hard surface cleaning in the context of the present invention can include removing heavy soiling, removing slight soiling and removing dust, even removing small quantities of dust.
• soiling to be removed are not limited to dust and soil but can be soot, hydrocarbons, e.g., oil, engine oil, furthermore residues from food, drinks, body fluids such as blood or excrements, furthermore complex natural mixtures such as grease, and complex synthetic mixtures such as paints, coatings, and pigment containing grease.
• hydrocarbons e.g., oil, engine oil
• body fluids such as blood or excrements
• complex natural mixtures such as grease
• complex synthetic mixtures such as paints, coatings, and pigment containing grease.
• the contacting of the hard surface with inventive formulation can be performed once or repeatedly, for example twice or three times.
• inventive formulation containing soil or dust After having performed the contacting the hard surface with inventive formulation the remaining inventive formulation containing soil or dust will be removed. Such removal can be effected by removal of the object with the now clean hard surface from the respective inventive formulation or vice versa, and it can be supported by one or more rinsing step(s).
• the object with the now-clean hard surface can be dried. Drying can be effected at room temperature or at elevated temperature such as, e.g., 35 to 95°C. Drying can be performed in a drying oven, in a tumbler (especially with fibers and with fabrics), or in a stream of air having room temperature or elevated temperature such as 35 to 95°C. Freeze-drying is another option.
• hard surfaces can be cleaned very well. In particular, objects with structured hard surfaces can be cleaned well.
• a further aspect of the present invention is a process of making inventive formulations, briefly also being referred to as inventive process.
• inventive process comprises the step of mixing at least one compound of general formula (I) and optionally with at least one active ingredient, preferably selected from organic complexing agents, anionic surfactants and organic acids, selected from acetic acid, citric acid, and methanesulfonic acid.
• active ingredient preferably selected from organic complexing agents, anionic surfactants and organic acids, selected from acetic acid, citric acid, and methanesulfonic acid.
• Mixing can be achieved, e. g., by stirring the ingredients into water. After mixing, the water can be removed in whole or in part by, e.g., spray drying.
• Mixing can be achieved, e. g., at ambient temperature or at slightly elevated temperature, for example in the range of from 30 to 45°C.
• a further aspect of the present invention is a compound of general formula (I) wherein the integers R 1 are different or identical and selected from C3-Cio-alkyl groups with at least two methyl groups per R 1 ,
• YH is (AO)n-H, with AO being selected from -CH 2 CH 2 0- and -CH 2 CH(R 2 )0- and being different or identical in the case of n > 1 ,
• R 2 being different or identical and selected from Ci-Ci6-alkyl, branched or linear, n in the range of from 1 to 30,
• polydispersity being in the range of from 1.0 to 1.5.
• the polydispersity (M w /M n ) of inventive compound according to general formula (I) is in the range of from 1.0 to 1 .5.
• the integers and their preferred embodiments are defined in more detail above.
• R 1 is a CH(CH3)2-group.
• inventive compounds can advantageously be used for making inventive formulations.
• inventive compounds may contain compounds of general formula (III) as an impurity, said impurity also being referred to as residual alcohols.
• inventive mixtures contain in the range of from 100 ppm to 1 % b weight of residual alcohols.
• a further aspect of the present invention is a process for making an inventive mixture, briefly also referred to as inventive synthesis, comprising the step of reacting the corresponding alcohol according to formula (III) with R 1 being defined as above, with at least one alkylene oxide selected from ethylene oxide and alkylene oxides according to formula (II)
• R 2 being different or identical and selected from Ci-Ci6-alkyl, branched or linear, in the presence of at least one catalyst, selected from double-metal cyanides.
• the integers are defined as above.
• Double-metal cyanides hereinafter also referred to as double-metal cyanide compounds or DMC compounds, usually comprise at least two different metals, at least one of them being selected from transition metals and the other one being selected from transition metals and alkali earth metals, and furthermore cyanide counterions.
• Particularly suitable catalysts for the alkoxy- lation are double-metal cyanide compounds which contain zinc, cobalt or iron or two thereof. Berlin blue, for example, is particularly suitable.
• crystalline DMC compounds Preference is given to using crystalline DMC compounds.
• a crystal- line DMC compound of the Zn-Co type which comprises zinc acetate as further metal salt component is used as catalyst.
• Such compounds crystallize in monoclinic structure and have a platelet-like habit.
• Such compounds are described, for example, in WO 00/74845 and in WO 01/64772.
• Examples of double-metal cyanide compounds suitable as catalyst are described in WO
• Double-metal cyanide compounds can be used as powder, paste or suspension or be moulded to give a moulding, be introduced into mouldings, foams or the like or be applied to mouldings, foams or the like.
• the double-metal cyanide compound concentration used for the inventive synthesis, based on the alcohol according to general formula (III), is preferably less than 2000 ppm (i.e. mg of cata- lyst per kg of product), more preferably less than 1000 ppm, in particular less than 500 ppm, particularly preferably less than 100 ppm, for example less than 50 ppm or 35 ppm, particularly preferably less than 25 ppm; ppm referring to mass-ppm (parts per million) of compound of general formula (III).
• the inventive synthesis is carried out at temperatures in the range of from 90 to 240°C, preferably from 120 to 180°C, in a closed vessel.
• ethylene oxide or alkylene oxide of general formula (III) or a mixture of different alkylene oxides of general formula (III) or a mixture of ethylene oxide and alkylene oxide of general formula (III) can also generally be referred to as "alkylene ox- ide(s)".
• alkylene oxide(s) is/are introduced into a mixture of compound of general formula (III) and double-metal cyanide compound under the vapour pres- sure of the alkylene oxide(s) prevailing at the selected reaction temperature.
• Alkylene oxide(s) can be introduced in pure form or, as an alternative, be diluted up to about 30 to 60% by volume with an inert gas such as a rare gas or nitrogen. This affords additional safety against explosionlike polyaddition of the alkylene oxide.
• polyether chains will be formed in which the different alkylene oxide units are distributed virtually randomly in compounds of general formula (I).
• Variations in the distribution of the units along the polyether chain can arise due to differing reaction rates of the alkylene oxides. Variations in the distribution of the units along the polyether chain can be achieved arbitrarily by continuously introducing an alkylene oxide mix- ture of program-controlled composition as well. In case different alkylene oxides are reacted subsequently, then polyether chains with a block-type distribution of the alkylene oxide units are obtained. In another embodiment with different alkylene oxides being reacted, addition of one alkylene oxide is being started before the other alkylene oxide has been completely reacted.
• Preferred inventive mixtures can be obtained by reacting compound of general formula (III) firstly with propylene oxide and then with ethylene oxide under conditions indicated above. Further preferred inventive mixtures can be obtained by reacting compound of general formula (III) solely with ethylene oxide.
• the inventive synthesis is carried out without a dil- uent or solvent.
• the inventive synthesis can be carried out using a solvent.
• Suitable solvents are, for example, ⁇ , ⁇ -dimethyl formamide, toluene, xylene, and mixtures of toluene and xylene, or solvent naphtha.
• the inventive synthesis is carried out in a way that a reaction with alkoxide of general formula (II), especially with propylene oxide, is carried out first, followed by subsequent ethoxylation.
• a reaction with alkoxide of general formula (II), especially with propylene oxide is carried out first, followed by subsequent ethoxylation.
• the content of residual alcohol in the alkoxylates can be reduced, it being observed that propylene oxide is reacted more evenly with compound of general formula (III).
• alkylene oxide(s) is incomplete with respect to al- kylene oxide(s).
• alkylene oxide(s) is/are reacted in a molar excess of at least 1 .5 ⁇ n, referring to the total of compound according to general formula (III).
• the inventive synthesis is carried out in the presence of at least one double-metal cyanide selected from hexacyano cobaltates.
• the inventive synthesis is carried out in the pres- ence of at least one double-metal cyanide selected from compounds according to general formula (VI)
• M 1 is at least one metal ion chosen from the group consisting of Zn 2+ , Fe 2+ , Fe 3+ , Co 3+ , Ni 2+ , Mn 2+ , Co 2+ , Sn2 + , Pb 2+ , Mo 4+ , Mo 6+ , Al 3+ , V 4+ , V 5+ , Sr 2+ , W 4+ , W 6+ , Cr 2+ , Cr 3+ , Cd 2+ , Hg 2+ , Pd 2+ , Pt 2+ , V 2+ , Mg 2+ , Ca 2+ , Ba 2+ , Cu 2+ , La 3+ , Ce 3+ , Ce 4+ , Eu 3+ , Ti 3+ , Ti 4+ , Ag + , Rh 2+ , Rh 3+ , Ru 2+ , Ru 3+ ,
• M 2 is at least one metal ion chosen from the group consisting of Fe 2+ , Fe 3+ , Co 2+ , Co 3+ , Mn 2+ , Mn 3+ , V 4+ , V 5+ , Cr 2+ , Cr 3+ , Rh 3+ , Ru 2+ , lr 3+ , and in a way that M 1 and M 2 are not identical,
• a and X independently of one another, are anions selected from the group consisting of halide, hydroxide, sulfate, carbonate, cyanide, thiocyanate, isocyanate, cyanate, carboxylate, oxalate, nitrate, nitrosyl, hydrogensulfate, phosphate, dihydrogenphosphate, hydrogenphosphate or hy- drogencarbonate,
• L is a ligand chosen from the group consisting of alcohols, aldehydes, ketones, ethers, polyeth- ers, esters, polyesters, polycarbonate, ureas, amides, primary, secondary and tertiary amines, ligands with pyridine nitrogen, nitriles, sulfides, phosphides, phosphites, phosphanes, phospho- nates and phosphates, k is an integer greater than or equal to zero, and up to 6. The integer k can be a whole number or a fraction.
• P is an organic additive
• a, b, c, d, g and n are chosen such that the electroneutrality of the compound (VI) is ensured, where each f and c may be 0,
• e is the number of ligand molecules, for example a fraction or an integer greater than zero, or zero, f and h, independently of one another, are fractions or integers greater than zero, or zero.
• the upper limits of e, f, and h are 6.
• organic additive P is selected from polyethers, polyesters, polycarbonates, polyalkylene glycol sorbitan esters, polyalkylene glycol glycidyl ethers, polyacrylamide, poly(acrylamide-co-acrylic acid), polyacrylic acid, poly(acrylamide-co-maleic acid), polyacryloni- trile, polyalkyl acrylates, polyalkyl methacrylates, polyvinyl methyl ether, polyvinyl ethyl ether, polyvinyl acetate, polyvinyl alcohol, poly-N-vinylpyrrolidone, poly(N-vinylpyrrolidone-co-acrylic acid), polyvinyl methyl ketone, poly(4-vinylphenol), poly(acrylic acid-co-styrene), oxazoline pol- ymers, polyalkyleneimines, maleic acid and maleic anhydride copolymers, hydroxyethylcellu- lose, polyacetates
• Double-metal cyanide compounds may be crystalline or amorphous. When k is zero, crystalline double-metal cyanide compounds are preferred. When k is greater than zero, crystalline, partially crystalline and also substantially amorphous catalysts are preferred.
• a preferred embodiment covers catalysts of the formula (VI) in which k is greater than zero.
• the preferred catalyst then comprises at least one double-metal cyanide compound, at least one organic ligand and at least one organic additive P.
• k is zero, optionally e is also zero and X is exclusively a carboxylate, preferably formate, acetate and propionate.
• preference is given to crystalline double-metal cyanide catalysts.
• Other preferred embodiments are double-metal cyanide catalysts as described in WO 00/74845, which are crystalline and platelet-like.
• f, e and k do not equal zero.
• Such embodiments refer to double-metal cyanide catalysts which contain L, preferably in amounts of from
• Such catalysts can either be prepared with vigorous stirring (24,000 rpm using Turrax) or with stirring, as described in US 5,158,922.
• double-metal cyanide compounds can be are prepared by combining a metal salt solution with a cyanometallate solution, which may optionally contain both a ligand L and also an organic additive P. Subsequently, the organic ligand and optionally the organic additive are added.
• a metal salt solution with a cyanometallate solution, which may optionally contain both a ligand L and also an organic additive P.
• the organic ligand and optionally the organic additive are added.
• an inactive double-metal cyanide compound is firstly prepared, and this is then converted into its active phase by recrystallization, as described in WO 01/64772.
• DMC compounds suitable as catalysts may, in principle, be prepared by all ways known to the person skilled in the art.
• the DMC compounds can be prepared by direct precipitation, incipient wetness method, by preparing a precursor phase and subsequent recrystallization.
• the reaction mixture can be filtered, e.g., over cellulose filter material, or degassed under reduced pressure.
• reduced pressure may mean, e.g., 10 to 50 mbar at a temperature in the range of from 30 to 100°C.
• inventive compounds can be obtained in excellent yields.
• the present invention is further illustrated by working examples.
• the following catalyst was used: Zn3[Co(CN)6]2 -ZnC -FbO, commercially available as Arcol Catalyst 3.
• a 2-liter autoclave with anchor stirrer was charged with 189.8 g (1.2 mol) of 2-isopropyl-5- methylhexan-1 -ol and 0.61 g of catalyst.
• the resultant mixture was heated under stirring (100 rpm) to 80°C, and flushed 3 times with dry nitrogen.
• a pressure of 1.5 bar was set by introducing dry nitrogen.
• the temperature was raised to 130°C.
• a total of 422 g (9.6 moles) of ethylene oxide were introduced, distributed in three portions.
• the mixture was stirred for another 6 hours at 130°C. Then, the mixture was cooled down to 80°C and flushed three times with nitrogen. It was then degassed at 100°C/20 mbar. Then, the mixture was filtered over a cellulose filter.
• the resultant inventive compound (1.1 ) was a white solid at ambient temperature.
• the yield was almost quantitative.
• the residual alcohol content was 0.5% by weight.
• the polydispersity was determined by gel permeation chromatography (GPC), with tetrahydro- furan (THF) as eluent.
• a 2-liter autoclave with anchor stirrer was charged with 189.8 g (1 .2 mol) of 2-isopropyl-5- methylhexan-1 -ol and 0.61 g of catalyst.
• the resultant mixture was heated under stirring (100 rpm) to 80°C, and flushed 3 times with dry nitrogen.
• a pressure of 1.5 bar was set by introducing dry nitrogen.
• the temperature was raised to 130°C.
• 104.6 g (1 .8 mol) of propylene oxide and a total of 422 g (9.6 moles) of ethylene oxide were introduced subsequently, the ethylene oxide being distributed in two portions. At first, the propylene was introduced. Then a first portion, 50 g, of ethylene oxide were introduced.
• the mixture was stirred for another 6 hours at 130°C. Then, the mixture was cooled down to 80°C and flushed three times with nitrogen. It was then degassed at 100°C/20 mbar. Then, the mixture was filtered over a cellulose filter.
• the resultant inventive compound (1.2) was a white solid at ambient temperature.
• the yield was almost quantitative.
• the residual alcohol content was 0.5% by weight.
• the order of addition was as follows: First, a bucket was charged with demineralized water. Then, under stirring, compound (1.1 ) or (I.2) was added - or, in case of comparative examples, surfactants (C-VII.1 ) or (C-VII.2). Then, further ingredients according to table 3 were added, the last one being citric acid to adjust the pH value to 3. The respective bathroom cleaners were obtained as clear, homogeneous liquids.
• Kitchen tiles were tiles with a color acceptable in a kitchen.
• a standard soil was prepared, by mixing 25 g butter, 25 g lard, 25 g margarine, 12.5 g ketchup, and 12.5 mustard in a beaker on a water bath at 40 to 45°C under continuous stirring. Then, a roller was dipped into the soil so obtained and about 3 g of the soil were applied to a pre- cleaned (ethanol) kitchen tiles. Then, the standard soil was evenly distributed on the kitchen tiles and the kitchen tiles then dried in an oven (180°C, 2 hours). They were then allowed to cool to ambient temperature. Soiled tiles were obtained. Kitchen cleaners according to table 1 were filled into 4 different trigger dispensers.
• Each two soiled tiles were selected, and each of them sprayed with kitchen cleaner: the left half of the surface of the first soiled tile was sprayed with 3.5 g of IF.1 and the right half with C-F.4. The left half of the surface of the second soiled tile was sprayed with 3.5 g of IF.2 and the right half with C-F.3.
• the kitchen cleaners were allowed to rest for 2 minutes. Then, the different parts were wiped with cellulose type wet sponges without using force. Then, the kitchen cleaners were removed by rinsing with cold tap water.
• the experiment was repeated 4 times, with fresh soiled tiles. The removal of the soil was assessed visually.

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